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小鼠成纤维细胞通过胚胎干细胞提取物被重编程为表达Oct-4和Rex-1基因并具有碱性磷酸酶活性。

Mouse fibroblasts are reprogrammed to Oct-4 and Rex-1 gene expression and alkaline phosphatase activity by embryonic stem cell extracts.

作者信息

Neri Tui, Monti Manuela, Rebuzzini Paola, Merico Valeria, Garagna Silvia, Redi Carlo Alberto, Zuccotti Maurizio

机构信息

Laboratorio di Biologia dello Sviluppo, Dipartimento di Biologia Animale, Universita' di Pavia, Italy.

出版信息

Cloning Stem Cells. 2007 Fall;9(3):394-406. doi: 10.1089/clo.2006.0011.

DOI:10.1089/clo.2006.0011
PMID:17907950
Abstract

A recent remarkable study has shown that when mouse NIH-3T3 fibroblasts are exposed to an embryonic stem cell (ESC) extract, the majority of them expresses the Oct-4 gene, form ESC-like colonies, and embryoid-like bodies that differentiate into cells of the three germ layers. The use of cell extracts for inducing cell dedifferentiation could be a powerful system to obtain large quantities of pluripotent cells. It is thus of crucial importance that the robustness of this method of cell transdifferentiation is tested by other laboratories before it is advanced to a more ambitious use in cell therapy programs. We report here our experimental observations using the same reprogramming protocol on STO and NIH-3T3 mouse fibroblasts. Three are the main results: first, we confirmed an enduring reprogramming activity of the ESC extract, although on a much smaller number of cells that varies from approximately 0.003 to 0.04% of the total population of fibroblasts and with an effect limited to the induction of Oct-4 and Rex-1 gene expression and alkaline phosphatase activity. Second, the expression of OCT-4, SSEA-1, and Forssman antigen proteins was never detected. Third, our work has clearly demonstrated that ESCs may survive the procedure of extract preparation, may be source of contamination that is expanded in culture and give false positive results.

摘要

最近一项引人注目的研究表明,当小鼠NIH-3T3成纤维细胞暴露于胚胎干细胞(ESC)提取物时,它们中的大多数会表达Oct-4基因,形成ESC样集落以及胚状体样结构,并分化为三个胚层的细胞。利用细胞提取物诱导细胞去分化可能是获得大量多能细胞的强大系统。因此,在将这种细胞转分化方法推进到细胞治疗计划中更宏大的应用之前,由其他实验室测试该方法的稳健性至关重要。我们在此报告我们使用相同重编程方案对STO和NIH-3T3小鼠成纤维细胞进行实验的观察结果。主要有三个结果:第一,我们证实了ESC提取物具有持久的重编程活性,尽管作用于数量少得多的细胞,这些细胞约占成纤维细胞总数的0.003%至0.04%,且其作用仅限于诱导Oct-4和Rex-1基因表达以及碱性磷酸酶活性。第二,从未检测到OCT-4、SSEA-1和福斯曼抗原蛋白的表达。第三,我们的工作清楚地表明,胚胎干细胞可能在提取物制备过程中存活下来,可能是培养中扩增的污染源并产生假阳性结果。

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